Suppr超能文献

甲磺酸伊马替尼:胃肠道间质瘤治疗的既往成就与未来挑战。

Imatinib mesylate: past successes and future challenges in the treatment of gastrointestinal stromal tumors.

机构信息

Medical Oncologist, Victoria Island Cancer Center, Victoria, British Columbia, Canada, 2410 Lee Avenue V8R 6V5.

出版信息

Clin Med Insights Oncol. 2011;5:365-79. doi: 10.4137/CMO.S4259. Epub 2011 Nov 9.

Abstract

Just over a decade ago, gastrointestinal tumours were a poorly understood mesenchymal neoplasm unsuccessfully treated with chemotherapy. Cytotoxic therapy for advanced disease yielded response rates of 10% and median survival of just 18 months. However, the discovery of KIT and platelet derived growth factor receptor alpha (PDGFRA) mutations as oncogenic drivers of most gastrointestinal tumours, paved the way for targeted therapy. Imatinib mesylate, a tyrosine kinase inhibitor, produces a clinical benefit rate (complete response, partial response, and stable disease) of more than 80% in metastatic setting and a median survival of 57 months. Imatinib is now also approved in adult patients following resection of KIT-positive GIST. Major insights into the mechanism of action of imatinib, unique pharmacokinetics, drug resistance, and management of low grade but chronic adverse effects continue to be made.

摘要

就在十多年前,胃肠道肿瘤是一种了解甚少的间叶性肿瘤,用化疗治疗效果不佳。晚期疾病的细胞毒性治疗的反应率为 10%,中位生存期仅为 18 个月。然而,发现 KIT 和血小板衍生生长因子受体α(PDGFRA)突变是大多数胃肠道肿瘤的致癌驱动因素,为靶向治疗铺平了道路。甲磺酸伊马替尼是一种酪氨酸激酶抑制剂,在转移性环境中产生超过 80%的临床受益率(完全缓解、部分缓解和稳定疾病),中位生存期为 57 个月。甲磺酸伊马替尼现在也被批准用于 KIT 阳性 GIST 切除后的成年患者。对伊马替尼作用机制、独特药代动力学、耐药性以及对低级别但慢性不良反应的管理的主要认识仍在不断取得进展。

相似文献

1
Imatinib mesylate: past successes and future challenges in the treatment of gastrointestinal stromal tumors.
Clin Med Insights Oncol. 2011;5:365-79. doi: 10.4137/CMO.S4259. Epub 2011 Nov 9.
2
Imatinib mesylate: in the treatment of gastrointestinal stromal tumours.
Drugs. 2003;63(5):513-22; discussion 523-4. doi: 10.2165/00003495-200363050-00005.
3
Molecular basis for primary and secondary tyrosine kinase inhibitor resistance in gastrointestinal stromal tumor.
Cancer Chemother Pharmacol. 2011 Jan;67 Suppl 1(Suppl 1):S25-43. doi: 10.1007/s00280-010-1526-3. Epub 2010 Nov 30.
4
Gastrointestinal stromal tumors.
Curr Top Microbiol Immunol. 2012;355:41-57. doi: 10.1007/82_2011_161.
5
[The importance of mutational status in prognosis and therapy of GIST].
Recenti Prog Med. 2015 Jan;106(1):17-22. doi: 10.1701/1740.18950.
6
[Clinicopathological features and prognosis of gastrointestinal stromal tumors with gene "homozygous mutation": a multicenter retrospective cohort study].
Zhonghua Wei Chang Wai Ke Za Zhi. 2021 Sep 25;24(9):804-813. doi: 10.3760/cma.j.cn.441530-20210720-00293.
8
Developments in targeted therapy of advanced gastrointestinal stromal tumors.
Recent Pat Anticancer Drug Discov. 2008 Jun;3(2):88-99. doi: 10.2174/157489208784638749.

引用本文的文献

1
Clinical Use of Liquid-Based Comprehensive Genomic Profiling in Gastrointestinal Stromal Tumors.
Lab Invest. 2025 May;105(5):104116. doi: 10.1016/j.labinv.2025.104116. Epub 2025 Feb 19.
2
Precision Oncology in Gastrointestinal Stromal Tumors.
Curr Oncol. 2023 Apr 30;30(5):4648-4662. doi: 10.3390/curroncol30050351.
3
Tumour lysis syndrome: a rare side effect of imatinib therapy for GIST.
BMJ Case Rep. 2018 Nov 28;11(1):e226647. doi: 10.1136/bcr-2018-226647.
5
Conformational landscape and low lying excited states of imatinib.
J Mol Model. 2015 Apr;21(4):84. doi: 10.1007/s00894-015-2639-8. Epub 2015 Mar 13.
6
Assessment of tracer 99mTc(V)-DMSA uptake as a measure of tumor cell proliferation in vitro.
PLoS One. 2013;8(1):e54361. doi: 10.1371/journal.pone.0054361. Epub 2013 Jan 15.
7
Targeted therapy in rare cancers--adopting the orphans.
Nat Rev Clin Oncol. 2012 Nov;9(11):631-42. doi: 10.1038/nrclinonc.2012.160. Epub 2012 Sep 11.
8
Imatinib mesylate causes genome-wide transcriptional changes in systemic sclerosis fibroblasts in vitro.
Clin Exp Rheumatol. 2012 Mar-Apr;30(2 Suppl 71):S86-96. Epub 2012 May 29.

本文引用的文献

1
The safety profile of imatinib in CML and GIST: long-term considerations.
Arch Toxicol. 2012 Jan;86(1):1-12. doi: 10.1007/s00204-011-0729-7. Epub 2011 Jun 30.
2
Nilotinib: a novel, selective tyrosine kinase inhibitor.
Semin Oncol. 2011 Apr;38 Suppl 1(0 1):S3-9. doi: 10.1053/j.seminoncol.2011.01.016.
4
Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations.
Proc Natl Acad Sci U S A. 2011 Jan 4;108(1):314-8. doi: 10.1073/pnas.1009199108. Epub 2010 Dec 20.
5
Molecular basis for primary and secondary tyrosine kinase inhibitor resistance in gastrointestinal stromal tumor.
Cancer Chemother Pharmacol. 2011 Jan;67 Suppl 1(Suppl 1):S25-43. doi: 10.1007/s00280-010-1526-3. Epub 2010 Nov 30.
7
Response assessment in gastrointestinal stromal tumor.
Int J Cancer. 2011 Mar 15;128(6):1251-8. doi: 10.1002/ijc.25729. Epub 2011 Jan 7.
8
Periorbital edema secondary to imatinib mesylate.
Clin Ophthalmol. 2010 May 14;4:427-31. doi: 10.2147/opth.s8521.
9
Immunohistochemistry for SDHB divides gastrointestinal stromal tumors (GISTs) into 2 distinct types.
Am J Surg Pathol. 2010 May;34(5):636-44. doi: 10.1097/PAS.0b013e3181d6150d.
10
Heat shock proteins as targets in oncology.
Clin Transl Oncol. 2010 Mar;12(3):166-73. doi: 10.1007/s12094-010-0486-8.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验